| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:6367642-6367835 | Rare:38 | ||||
| chr18:6414833-6414990 | Rare:62 | ||||
| chr18:6729728-6729970 | Rare:65 | ||||
| chr18:7117682-7117905 | Common:3; Rare:79 | ||||
| chr18:7567148-7567467 | Common:5; Rare:83 | ||||
| chr18:7946856-7946898 | Rare:4 | ||||
| chr18:8707634-8707861 | Rare:42 | ||||
| chr18:9102459-9102780 | Common:2; Rare:133; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136578-9137076 | Common:1; Rare:187 | ||||
| chr18:9137162-9137363 | Common:1; Rare:70 | ||||
| chr18:9334428-9334871 | Common:1; Rare:108 | ||||
| chr18:9474819-9475060 | Common:1; Rare:59 | ||||
| chr18:9475200-9475666 | Common:7; Rare:128 | ||||
| chr18:9614480-9614994 | Common:2; Rare:173 | ||||
| chr18:9615030-9615123 | Rare:28 |